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Parents of a child with a chronic illness can experience greater distress than the average population, yet little is understood about differences between illness groups. This cross-sectional survey study aimed to compare parents’ psychological distress and perceived wellbeing across five chronic illnesses. Parents from one Australian pediatric hospital completed the Kessler Psychological Distress Scale and seven purpose-designed items about their wellbeing. Data from 106 parents (cancer = 48, cystic fibrosis CF = 27, kidney disease = 12, gastrointestinal condition/disorder = 9, developmental and epileptic encephalopathy DEE = 10) was analysed using bivariate Pearson’s Correlation and linear mixed-effects models. Parents’ distress scores differed between groups ( F(4,80) = 2.50, p = .049), with the DEE group reporting higher distress than the CF group ( mean difference = 6.76, 95% CI 0.11, 13.42). Distress scores were moderately correlated to parents’ perceptions of their child’s health and their own wellbeing. Parents’ self-reported coping with their child’s condition/treatments differed ( F(4,81) = 3.24, p = .016), with the DEE group rating their coping as poorer than the CF group ( mean difference = −25.32, 95% CI −46.52, 4.11). Across all groups, parents reported unmet needs, particularly for psychosocial support and practical/financial assistance. Support interventions may be most effective if tailored to the child’s illness, with greater support potentially needed for parents who have a child with DEE and/or severe comorbidities.
Robertson et al. (Fri,) studied this question.